NDC 14505-398

Sanatos Day

Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine

Sanatos Day is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Pharmalab Enterprises Inc. The primary component is Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine.

• Product ID: 14505-398_cb6c6e0c-0ae5-4c15-bbe2-0c2801106723
• NDC: 14505-398
• Product Type: Human Otc Drug
• Proprietary Name: Sanatos Day
• Generic Name: Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2010-02-04
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Pharmalab Enterprises Inc
• Substance Name: ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE
• Active Ingredient Strength: 325 mg/15mL; mg/15mL; mg/15mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 14505-398-06

177 mL in 1 BOTTLE, PLASTIC (14505-398-06)

• Marketing Start Date: 2010-02-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 14505-398-06 [14505039806]

Sanatos Day LIQUID

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-02-04
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	325 mg/15mL

OpenFDA Data

• SPL SET ID: 952273e7-84aa-41ac-87ca-b947fdf20fa9
• Manufacturer:
  • Pharmalab Enterprises Inc
• UNII:
  • 362O9ITL9D
  • 9D2RTI9KYH
  • 1WS297W6MV
• RxNorm Concept Unique ID - RxCUI:
  • 1113705

NDC Crossover Matching brand name "Sanatos Day" or generic name "Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine"

NDC	Brand Name	Generic Name
68016-598	Daytime Cold and Flu Relief	Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine
14505-398	Sanatos	Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine